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1.
J Pediatr Rehabil Med ; 7(3): 255-65, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-25260508

RESUMO

PURPOSE: Respiratory muscle weakness is a primary therapeutic challenge for patients with infantile Pompe disease. We previously described the clinical implementation of a respiratory muscle training (RMT) regimen in two adults with late-onset Pompe disease; both demonstrated marked increases in inspiratory and expiratory muscle strength in response to RMT. However, the use of RMT in pediatric survivors of infantile Pompe disease has not been previously reported. METHOD: We report the effects of an intensive RMT program on maximum inspiratory pressure (MIP) and maximum expiratory pressure (MEP) using A-B-A (baseline-treatment-posttest) single subject experimental design in two pediatric survivors of infantile Pompe disease. Both subjects had persistent respiratory muscle weakness despite long-term treatment with alglucosidase alfa. RESULTS: Subject 1 demonstrated negligible to modest increases in MIP/MEP (6% increase in MIP, d=0.25; 19% increase in MEP, d=0.87), while Subject 2 demonstrated very large increases in MIP/MEP (45% increase in MIP, d=2.38; 81% increase in MEP, d=4.31). Following three-month RMT withdrawal, both subjects maintained these strength increases and demonstrated maximal MIP and MEP values at follow-up. CONCLUSION: Intensive RMT may be a beneficial treatment for respiratory muscle weakness in pediatric survivors of infantile Pompe disease.


Assuntos
Exercícios Respiratórios , Doença de Depósito de Glicogênio Tipo II/fisiopatologia , Doença de Depósito de Glicogênio Tipo II/reabilitação , Músculos Respiratórios/fisiologia , Resistência das Vias Respiratórias/fisiologia , Criança , Expiração/fisiologia , Humanos , Inalação/fisiologia , Pulmão/fisiopatologia , Contração Muscular/fisiologia
2.
Mol Genet Metab ; 104(3): 417-20, 2011 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-21641843

RESUMO

Respiratory muscle strength training (RMST) is an exercise-based intervention which targets respiratory muscle weakness. We implemented RMST in two patients with late-onset Pompe disease (LOPD), both who had received long-term enzyme replacement therapy and had severe respiratory weakness. Over 16-32 weeks, inspiratory muscle strength increased by 73-74%. Expiratory muscle strength increased 31-48% over 12-22 weeks. These findings suggest that RMST may increase respiratory muscle strength, even in the setting of LOPD and severe baseline weakness.


Assuntos
Doença de Depósito de Glicogênio Tipo II/reabilitação , Força Muscular/fisiologia , Treinamento Resistido/métodos , Músculos Respiratórios/fisiologia , Expiração/fisiologia , Feminino , Doença de Depósito de Glicogênio Tipo II/tratamento farmacológico , Humanos , Inalação/fisiologia , Masculino , Pessoa de Meia-Idade , alfa-Glucosidases/uso terapêutico
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